Evidence map›Paper›PMID 27812114›Full record

ArticlePLoS genetics2016

A Mutational Hotspot and Strong Selection Contribute to the Order of Mutations Selected for during Escherichia coli Adaptation to the Gut.

Marta Lourenço, Ricardo S Ramiro, Daniela Güleresi, João Barroso-Batista, Karina B Xavier, Isabel Gordo, Ana Sousa

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Predicting the effect of mutations to investigate recent events of selection across 60,472Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Shared Evolutionary Path in Social Microbiomes.Molecular biology and evolution · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Evolutionary stalling and a limit on the power of natural selection to improve a cellular module.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Horizontal gene transfer overrides mutation inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Article
  19. Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Marta LourençoInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Ricardo S RamiroInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID http://orcid.org/0000-0002-4834-6997
Daniela GüleresiInstituto Gulbenkian de Ciência, Oeiras, Portugal.
João Barroso-BatistaInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Karina B XavierInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID http://orcid.org/0000-0001-5210-1434
Isabel GordoInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Ana SousaInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID http://orcid.org/0000-0002-7276-4195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The relative role of drift versus selection underlying the evolution of bacterial species within the gut microbiota remains poorly understood. The large sizes of bacterial populations in this environment suggest that even adaptive mutations with weak effects, thought to be the most frequently occurring, could substantially contribute to a rapid pace of evolutionary change in the gut. We followed the emergence of intra-species diversity in a commensal Escherichia coli strain that previously acquired an adaptive mutation with strong effect during one week of colonization of the mouse gut. Following this first step, which consisted of inactivating a metabolic operon, one third of the subsequent adaptive mutations were found to have a selective effect as high as the first. Nevertheless, the order of the adaptive steps was strongly affected by a mutational hotspot with an exceptionally high mutation rate of 10-5. The pattern of polymorphism emerging in the populations evolving within different hosts was characterized by periodic selection, which reduced diversity, but also frequency-dependent selection, actively maintaining genetic diversity. Furthermore, the continuous emergence of similar phenotypes due to distinct mutations, known as clonal interference, was pervasive. Evolutionary change within the gut is therefore highly repeatable within and across hosts, with adaptive mutations of selection coefficients as strong as 12% accumulating without strong constraints on genetic background. In vivo competitive assays showed that one of the second steps (focA) exhibited positive epistasis with the first, while another (dcuB) exhibited negative epistasis. The data shows that strong effect adaptive mutations continuously recur in gut commensal bacterial species.

Indexed as

Epistasis, GeneticAdaptation, PhysiologicalAllelesAnimalsDicarboxylic Acid TransportersEscherichia coliEscherichia coli ProteinsEvolution, MolecularGastrointestinal MicrobiomeGenetic VariationMembrane Transport ProteinsMiceMutationSelection, GeneticdcuB protein, E coliDicarboxylic Acid TransportersEscherichia coli ProteinsFocA protein, E coliMembrane Transport Proteins

Identifiers

PMID27812114
PMCPMC5094792

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.